Canonical Allele Identifier: PA2825067397
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 956475
ClinVar RCV Id: RCV001229287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Tyr252Phe
CA340393588
NM_000098.3:c.755A>T